ELISA 1: 1,000. Immunohistochemistry 1: 50 - 1: 100. Other applications not tested. Optimal dilutions are dependent on conditions and should be determined by the user.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Liquid
Konzentration
0.25 mg/mL
Buffer
PBS with 0.09 % (W/V) sodium azide
Konservierungsmittel
Sodium azide
Vorsichtsmaßnahmen
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handhabung
Avoid repeated freezing and thawing.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer.
CX31 antikoerper, DFNA2 antikoerper, DFNA2B antikoerper, EKV antikoerper, Cnx31 antikoerper, Cx31 antikoerper, D4Wsu144e antikoerper, Gjb-3 antikoerper, ekv antikoerper, cx31 antikoerper, dfna2 antikoerper, gjb3b antikoerper, dfna2b antikoerper, connexin-31 antikoerper, gap junction protein beta 3 antikoerper, gap junction protein, beta 3 antikoerper, gap junction protein beta 3 L homeolog antikoerper, GJB3 antikoerper, Gjb3 antikoerper, gjb3.L antikoerper, gjb3 antikoerper
Hintergrund
Gap junctions are conduits that allow the direct cell-to-cell passage of small cytoplasmic molecules, including ions, metabolic intermediates, and second messengers, and thereby mediate intercellular metabolic and electrical communication. Gap junction channels consist of connexin protein subunits, which are encoded by a multigene family. GJBs (gap-junction proteins or connexins) play crucial functional roles associated with these channels. Defects in GJB3 have been linked to erythrokeratodermia variabilis (EKV) is an autosomal dominant genodermatosis characterized by transient figurate red patches or hyperkeratosis. Mutations in GJB2 have also been associated with genetically derived hearing impairments, including autosomal recessive nonsyndromic deafness.Synonyms: Connexin-31, Gap junction beta-3 protein